HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297607Generated: October 28, 2026
N-bromobutanimide → 7-Amino-8-bromo-2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinoline
https://huagongshe.com/reaction/2297607
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 18382547 | HCID 18382547 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Amino-8-bromo-2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinoline | HCID 18382561 | — |
Reaction Steps
To a solution of 7-amino-2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinoline from D3 (7 g) in acetonitrile (200 ml), was added N-bromo succinimide (7.21 g) portionwise over 10 min. The reaction mixture was cooled in an ice/methanol bath to prevent any large exotherm. and then stirred under argon for 45 min. The reaction was allowed to warm to 25° C., diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and evaporated to dryness in vacuo. The resultant brown solid was purified using dry flash column chromatography with ethyl acetate. Combination of appropriate fractions gave the title compound as an orange gum (3.95 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492378B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-f2961e842fcf43a081945c59f309fab6 |
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| Source note | uspto-grants-2002_12 |
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